FB2025_01 , released February 20, 2025
Allele: Dmel\mei-W68unspecified
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General Information
Symbol
Dmel\mei-W68unspecified
Species
D. melanogaster
Name
FlyBase ID
FBal0143327
Feature type
allele
Associated gene
Dmel\mei-W68
Associated Insertion(s)
Carried in Construct
Key Links
Allele class
Mutagen
    Nature of the Allele
    Allele class
    Mutagen
    Progenitor genotype
    Cytology
    Description
    Mutations Mapped to the Genome
    Curation Data
    Type
    Location
    Additional Notes
    References
    Variant Molecular Consequences
    Associated Sequence Data
    DDBJ / EMBL / GenBank
    DNA sequence
    Protein sequence
     
    UniProtKB/Swiss-Prot
      UniProtKB/TrEMBL
        Expression Data
        Reporter Expression
        Additional Information
        Statement
        Reference
         
        Marker for
        Reflects expression of
        Reporter construct used in assay
        Human Disease Associations
        Disease Ontology (DO) Annotations
        Models Based on Experimental Evidence ( 0 )
        Disease
        Evidence
        References
        Modifiers Based on Experimental Evidence ( 0 )
        Disease
        Interaction
        References
        Comments on Models/Modifiers Based on Experimental Evidence ( 0 )
         
        Disease-implicated variant(s)
         
        Phenotypic Data
        Phenotypic Class
        Phenotype Manifest In
        Detailed Description
        Statement
        Reference
        External Data
        Interactions
        Show genetic interaction network for Enhancers & Suppressors
        Phenotypic Class
        Phenotype Manifest In
        Additional Comments
        Genetic Interactions
        Statement
        Reference

        The eggshell defects seen in eggs derived from homozygous spn-D1 females are almost completely suppressed if the females are also homozygous for mei-W68unspecified; 98% of the eggshells are wild-type in eggs derived from double mutant females. The eggshell defects seen in eggs derived from spn-D1/spn-D2 females are completely suppressed if the females are also homozygous for mei-W68unspecified. The karyosome defects seen in spn-D1/spn-D2 egg chambers are also suppressed by mei-W68unspecified.

        (Abdu et al., 2003)

        The ovary phenotype of CSN5unspecified mutants is not suppressed by mei-W68unspecified.

        (Doronkin et al., 2003)

        The eggshell patterning defects of eggs derived from spn-B2/spn-BBU females are suppressed if the females also carry mei-W68unspecified/Df(2R)LL5. The eggshell patterning defects of eggs derived from mus301D4/mus301094 females are suppressed if the females also carry mei-W68unspecified/Df(2R)LL5. The eggshell patterning defects of eggs derived from okrRU/okrAA females are suppressed if the females also carry mei-W68unspecified/Df(2R)LL5.

        (Ghabrial and Schupbach, 1999)
        Xenogenetic Interactions
        Statement
        Reference
        Complementation and Rescue Data
        Comments
        Images (0)
        Mutant
        Wild-type
        Stocks (0)
        Notes on Origin
        Discoverer
        External Crossreferences and Linkouts ( 0 )
        Synonyms and Secondary IDs (1)
        Reported As
        Symbol Synonym
        mei-W68unspecified
        Name Synonyms
        Secondary FlyBase IDs
          References (4)